A genotyping system capable of simultaneously analyzing >1000 single nucleotide polymorphisms in a haploid genome.
about
A highly sensitive and specific system for large-scale gene expression profilingAccuTyping: new algorithms for automated analysis of data from high-throughput genotyping with oligonucleotide microarrays.Robust SNP genotyping by multiplex PCR and arrayed primer extension.An enhanced single base extension technique for the analysis of complex viral populations.Segmental duplication as one of the driving forces underlying the diversity of the human immunoglobulin heavy chain variable gene regionLOH analysis of genes around D4S2964 identifies ARD1B as a prognostic predictor of hepatocellular carcinomaEvidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate.Extensive analysis of D7S486 in primary gastric cancer supports TESTIN as a candidate tumor suppressor gene.Strong correlation between meiotic crossovers and haplotype structure in a 2.5-Mb region on the long arm of chromosome 21.Allele loss and down-regulation of heparanase gene are associated with the progression and poor prognosis of hepatocellular carcinoma.Comprehensive profiling of Epstein-Barr virus-encoded miRNA species associated with specific latency types in tumor cells.Long-range multilocus haplotype phasing of the MHCRapid high-resolution mapping of balanced chromosomal rearrangements on tiling CGH arrays.A novel approach for determining cancer genomic breakpoints in the presence of normal DNAAssociation of synapsin 2 with schizophrenia in families of Northern European ancestryAnalysis of genetic variations in CYP2C9, CYP2C19, CYP2D6 and CYP3A5 genes using oligonucleotide microarrayThe oncogene metadherin modulates the apoptotic pathway based on the tumor necrosis factor superfamily member TRAIL (Tumor Necrosis Factor-related Apoptosis-inducing Ligand) in breast cancer.Genetic structures of copy number variants revealed by genotyping single sperm.Identification of possible genetic alterations in the breast cancer cell line MCF-7 using high-density SNP genotyping microarray.RBM24 suppresses cancer progression by upregulating miR-25 to target MALAT1 in nasopharyngeal carcinoma.Improvements to bead-based oligonucleotide ligation SNP genotyping assays.Identification of a 7-gene signature that predicts relapse and survival for early stage patients with cervical carcinoma.Population Screening for Hemoglobinopathy Profiling: Is the Development of a Microarray Worthwhile?Identification of an 88-microRNA signature in whole blood for diagnosis of hepatocellular carcinoma and other chronic liver diseases.Tri-nucleotide threading for parallel amplification of minute amounts of genomic DNA.Identification of a gene-expression signature for predicting lymph node metastasis in patients with early stage cervical carcinoma.Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing.
P2860
Q28755360-33698233-5B79-4980-90F1-59F2790578EBQ31061489-5CBC1543-6E94-41AC-985D-D4640BD09529Q33317624-AB99504A-8ABD-440D-9192-85DEB9FF5D91Q33510938-825BBA27-5C26-4542-86F3-66C4B69A298EQ33805553-90FA1B9C-E7D8-4C45-B47B-2AFAD07C6F62Q33812222-25F2DF7D-3F2A-4520-964E-33533EEE3AE6Q33846861-611A1079-89AC-417A-BAF5-FB4E5689470BQ34043798-66DC9F00-79E2-49FC-B6E0-44CE37518DE3Q34338830-5155E095-3B65-4873-994A-6E304188C99FQ34406172-2709A61B-821B-4761-A591-4BF7E455EDD6Q34507851-D9863085-D686-4F4E-B457-994DB215A37CQ34598412-C0F91753-50F2-432B-93E2-8605F3151FD2Q35356418-D6C7F886-04DC-497A-A68C-34CA6F02422AQ35741860-E0A6AC27-6407-44BA-9929-17EEC0CEA81BQ36316351-7AE9E281-23DA-44A7-8AB3-98975ACF5991Q36412046-00515420-EE4B-4B0F-BDB4-3E534C5C3A63Q36725089-5602EF48-FC7F-4017-82FF-4E7758BF44B6Q37156529-500E0D3F-5E84-4F07-993B-D4486C22B05BQ37204031-C3C2D70E-EAAC-432C-A6AD-A391004354AAQ37330819-C84145F6-6E5B-49CE-AC9F-CD4073A47345Q37704894-54DDCCAA-43E8-4CBA-895F-9244D07C3B4BQ39660335-F969832E-9CAA-4A7C-B2DA-824D92AE29A3Q40724361-0E732F11-8338-4665-9576-D75944E52CF4Q41008487-139E58C5-0DE1-4F06-9E74-4E5AB8D34973Q43257119-FED73DAF-4E09-4404-A232-69B0FDB7C713Q44095909-DC423A81-6AED-47BE-A494-F66D168DAD1DQ54504446-A37707DF-D04E-4815-B8B8-D4995090D33B
P2860
A genotyping system capable of simultaneously analyzing >1000 single nucleotide polymorphisms in a haploid genome.
description
2005 nî lūn-bûn
@nan
2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
A genotyping system capable of ...... morphisms in a haploid genome.
@ast
A genotyping system capable of ...... morphisms in a haploid genome.
@en
type
label
A genotyping system capable of ...... morphisms in a haploid genome.
@ast
A genotyping system capable of ...... morphisms in a haploid genome.
@en
prefLabel
A genotyping system capable of ...... morphisms in a haploid genome.
@ast
A genotyping system capable of ...... morphisms in a haploid genome.
@en
P2093
P2860
P356
P1433
P1476
A genotyping system capable of ...... morphisms in a haploid genome.
@en
P2093
Danielle M Frikker
Guohong Hu
Honghua Li
Hui-Yun Wang
Irina V Tereshchenko
James Y Li
Manousos E Kambouris
Marco A Azaro
Minjie Luo
P2860
P304
P356
10.1101/GR.2885205
P577
2005-02-01T00:00:00Z